TY - JOUR
T1 - Unique features of transcription termination and initiation at closely spaced tandem human genes
AU - Nissani, Noa
AU - Ulitsky, Igor
N1 - We thank members of the Ulitsky lab for useful discussions and comments on the manuscript. This work was supported by grants to IU from the European Research Council (lncImpact project number 863589), the Abisch-Frenkel Foundation for the Promotion of Life Sciences, and the Kekst Family Institute for Medical Genetics. Author contributions Noa Nissani: Conceptualization; Data curation; Software; Formal analysis; Validation; Investigation; Visualization; Methodology; Writing—original draft; Writing—review and editing. Igor Ulitsky: Conceptualization; Data curation; Formal analysis; Supervision; Funding acquisition; Investigation; Writing—original draft; Project administration; Writing—review and editing. NN and IU conceived and designed the study. NN developed the computational pipelines and analyzed data under supervision of IU. NN and IU wrote the manuscript.
PY - 2022/4
Y1 - 2022/4
N2 - The synthesis of RNA polymerase II (Pol2) products, which include messenger RNAs or long noncoding RNAs, culminates in transcription termination. How the transcriptional termination of a gene impacts the activity of promoters found immediately downstream of it, and which can be subject to potential transcriptional interference, remains largely unknown. We examined in an unbiased manner the features of the intergenic regions between pairs of ‘tandem genes’—closely spaced (< 2 kb) human genes found on the same strand. Intergenic regions separating tandem genes are enriched with guanines and are characterized by binding of several proteins, including AGO1 and AGO2 of the RNA interference pathway. Additionally, we found that Pol2 is particularly enriched in this region, and it is lost upon perturbations affecting splicing or transcriptional elongation. Perturbations of genes involved in Pol2 pausing and R loop biology preferentially affect expression of downstream genes in tandem gene pairs. Overall, we find that features associated with Pol2 pausing and accumulation rather than those associated with avoidance of transcriptional interference are the predominant driving force shaping short tandem intergenic regions.
AB - The synthesis of RNA polymerase II (Pol2) products, which include messenger RNAs or long noncoding RNAs, culminates in transcription termination. How the transcriptional termination of a gene impacts the activity of promoters found immediately downstream of it, and which can be subject to potential transcriptional interference, remains largely unknown. We examined in an unbiased manner the features of the intergenic regions between pairs of ‘tandem genes’—closely spaced (< 2 kb) human genes found on the same strand. Intergenic regions separating tandem genes are enriched with guanines and are characterized by binding of several proteins, including AGO1 and AGO2 of the RNA interference pathway. Additionally, we found that Pol2 is particularly enriched in this region, and it is lost upon perturbations affecting splicing or transcriptional elongation. Perturbations of genes involved in Pol2 pausing and R loop biology preferentially affect expression of downstream genes in tandem gene pairs. Overall, we find that features associated with Pol2 pausing and accumulation rather than those associated with avoidance of transcriptional interference are the predominant driving force shaping short tandem intergenic regions.
UR - http://www.scopus.com/inward/record.url?scp=85127388799&partnerID=8YFLogxK
U2 - 10.15252/msb.202110682
DO - 10.15252/msb.202110682
M3 - مقالة
C2 - 35362230
SN - 1744-4292
VL - 18
JO - Molecular Systems Biology
JF - Molecular Systems Biology
IS - 4
M1 - e10682
ER -